ClinVar Miner

Submissions for variant NM_000368.4(TSC1):c.917G>A (p.Cys306Tyr) (rs752290177)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001086734 SCV000641678 benign Tuberous sclerosis 1 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000572956 SCV000675395 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-17 criteria provided, single submitter clinical testing Insufficient evidence
Athena Diagnostics Inc RCV000713912 SCV000844556 uncertain significance not provided 2017-09-11 criteria provided, single submitter clinical testing

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